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ALRN-6924 may prevent hair loss caused by chemotherapy.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

CTLA4 gene variants are not linked to alopecia areata in Monterrey's Mexican population.

The protein DDX6 helps keep skin cells renewing properly by controlling the production of certain other proteins and breaking down those that cause cells to mature too quickly.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

Two genetic variations in Moa buffalo help them adapt to heat.

The protein AtRXR3 limits root hair growth in Arabidopsis, affecting phosphorus uptake.

β-Catenin is essential for new hair growth after skin injury.

The Naked (N) trait in mice is linked to lower glycine and tyrosine in hair proteins.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

A 195 bp duplication in the HOXC10 gene causes crests in domestic chickens.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

K6hf is a unique protein found only in a specific layer of hair follicles.

The ABI1 gene contributes to prostate cancer progression and treatment resistance.

Researchers converted human embryonic stem cells into trophoblast stem cells using specific transcription factors.

BMP2 helps hair follicle stem cells become specialized by increasing PTEN, which causes autophagy.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

Trichorrhexis nodosa is mainly caused by hair trauma, not a metabolic defect.

TBX3 gene affects horse coat color, with higher expression in darker areas.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

The most common sign of aging at the gene level is more Ectodysplasin A2 Receptor (EDA2R) being made.

Combining genetic models helps improve heat tolerance in beef cattle.

Box A of HMGB1 can improve stem cell function, aiding anti-aging therapy.

TGF-β2 helps yak hair follicles enter the regression phase, while HSP70 tries to prevent it.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

TAGX-0003 protected hair follicles and reversed alopecia areata in a mouse model.

ROR2 is crucial for hair follicle stem cell maintenance and self-renewal.

Precise objectives can improve student achievement in health education.

A peptide from hair follicle stem cells can boost hair growth.